about
Palladium and organocatalysis: an excellent recipe for asymmetric synthesisEnantioconvergent catalysisPREPARATION OF (S)-tert-ButylPHOX (Oxazole, 4-(1,1-dimethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro- (4S)-)Enantioselective protonation.Mechanistic origin of the stereodivergence in decarboxylative allylationCatalytic enantioselective stereoablative reactions: an unexploited approach to enantioselective catalysisPREPARATION OF (S)-2-Allyl-2-methylcyclohexanone (Cyclohexanone, 2-methyl-2-(2-propen-1-yl)-, (2S)-).The Enantioselective Dakin-West Reaction.Asymmetric olefin isomerization of butenolides via proton transfer catalysis by an organic molecule.Synthesis and Exploration of Electronically Modified (R)-5,5-Dimethyl-(p-CF3)3-i-PrPHOX in Palladium-Catalyzed Enantio- and Diastereoselective Allylic Alkylation: A Practical Alternative to (R)-(p-CF3)3-t-BuPHOX.Intercepted Decarboxylative Allylations of Nitroalkanoates.Enantioselective Tsuji allylations.Regiospecific decarboxylative allylation of nitriles.Fluorine & chirality: how to create a nonracemic stereogenic carbon-fluorine centre?P,N ligands in asymmetric catalysis.Advances in Stereoconvergent Catalysis from 2005 to 2015: Transition-Metal-Mediated Stereoablative Reactions, Dynamic Kinetic Resolutions, and Dynamic Kinetic Asymmetric Transformations.Development of (trimethylsilyl)ethyl ester protected enolates and applications in palladium-catalyzed enantioselective allylic alkylation: intermolecular cross-coupling of functionalized electrophiles.Palladium-Catalyzed Asymmetric Alkylation in the Synthesis of Cyclopentanoid and Cycloheptanoid Core Structures Bearing All-Carbon Quaternary Stereocenters.A general enantioselective route to the chamigrene natural product family.A palladium-catalysed enolate alkylation cascade for the formation of adjacent quaternary and tertiary stereocentres.Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies.Rapid synthesis of an electron-deficient t-BuPHOX ligand: cross-coupling of aryl bromides with secondary phosphine oxides.Asymmetric Protonation of Cumulenolates: Synthesis of Allenyl Aldehydes Facilitated by an Organomanganese Auxiliary.Ruthenium catalyzed decarbonylative arylation at sp3 carbon centers in pyrrolidine and piperidine heterocycles.Homogeneous pd-catalyzed enantioselective decarboxylative protonation.The catalytic asymmetric total synthesis of elatol.The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation.Asymmetric fluorination of α-branched cyclohexanones enabled by a combination of chiral anion phase-transfer catalysis and enamine catalysis using protected amino acids.Direct, iridium-catalyzed enantioselective and regioselective allylic etherification with aliphatic alcohols.Enantioselective total synthesis of (+)-cassiol.Rhodium(I)-catalyzed redox-economic cross-coupling of carboxylic acids with arenes directed by N-containing groups.Chiral primary-amine-catalyzed conjugate addition to α-substituted vinyl ketones/aldehydes: divergent stereocontrol modes on enamine protonation.Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.Assembly of Terpenoid Cores by a Simple, Tunable Strategy.The Enantioselective Dakin-West ReactionA Stereoselective Switch: Enantiodivergent Approach to the Synthesis of Isoflavanones
P2860
Q26830862-5964347C-D5E9-4102-937C-F1CA07735E2FQ28077699-9E9D9D3E-BEDE-49E1-9611-0504F8DDF210Q33585051-06DC7653-F69D-40DA-8518-B6D8D7B1BFB9Q33812467-C2903829-C3A2-4E3F-952A-A4727BD01A68Q34034806-183A4C44-DB74-48E7-B88B-0DAB80DAF533Q34236967-79B66B4F-6307-4430-ADF9-7F64A4672725Q34445327-44657194-2093-44FA-8375-755F71F3B718Q34510563-8C267B70-BF13-4F15-BC47-241C155966E6Q35164377-990C4235-B345-4FC9-B07E-342A66540C54Q35915688-7AC1F4D9-8E4B-41C7-BD42-74EB9D32DAB4Q36197976-4846606C-3DA0-4C4C-BEE3-AD8F4448AA8DQ36970379-558E4C48-7E5F-4D2A-AFA0-83745BBB0CF1Q37479948-46E60632-6D06-426E-9C86-8735658A2C13Q37683482-BB62E312-CA35-4B0E-8A37-7BED9C9955F3Q38164480-670F5BC4-45FF-4BDD-B2CA-B953669358C9Q39121643-5E8DF7B0-7179-458B-B091-7F21FD0E8F51Q39284712-59B45231-DC88-4D1B-880D-98F3568AA20DQ41136502-012B3A86-3CAE-4B26-B777-4D1AF69585CBQ41788466-75CE30C0-AE6A-45D8-8A06-544A3BAE3C9AQ41878884-52BE7781-2197-4A7B-B83D-C8C0D51B612FQ42182848-551AB1C1-7E25-48A6-AA0D-CB5FD201F486Q42209265-B508ABDD-5E05-4FC9-BB9E-6F976E5B4ED9Q42380730-D1C51C80-C0F2-4823-B339-7DC66329257DQ42383756-A12EFCD0-6222-4F41-846F-D63F398717F2Q42394240-36933507-E4BF-4EC2-8987-2EFC2C048EACQ42434695-7D70AD44-22FD-4D31-B1AE-27C49A18E1C5Q42534222-D1996BB4-6807-42D5-90FF-1675167F8A1EQ42765042-FDEFDF0E-7A48-4855-94E7-BF543A091068Q42919978-396F0073-1D2A-4D58-8BAF-DF9DD4293CA1Q43098590-06E3395C-EDF0-4321-A1A6-C9C9A92987B6Q43717873-5773576B-8058-4BFA-BCCF-7C4A9CAF0329Q44244229-280815EF-E917-4F5E-B375-0F2899A99F8CQ46642667-F247AA04-6967-49EF-B295-3F2F1D2D9078Q48217297-418837EA-0207-4B16-99A0-27010B978DFFQ57742495-AF84FCC5-37CE-459D-9793-8B8E84F345A1Q58624078-F4A7F567-A861-4474-AE46-0A70C33B21CF
P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Catalytic enantioselective decarboxylative protonation.
@en
Catalytic enantioselective decarboxylative protonation.
@nl
type
label
Catalytic enantioselective decarboxylative protonation.
@en
Catalytic enantioselective decarboxylative protonation.
@nl
prefLabel
Catalytic enantioselective decarboxylative protonation.
@en
Catalytic enantioselective decarboxylative protonation.
@nl
P2093
P356
P1476
Catalytic enantioselective decarboxylative protonation.
@en
P2093
Brian M Stoltz
Douglas C Behenna
Toyoki Nishimata
P304
11348-11349
P356
10.1021/JA063335A
P407
P577
2006-09-01T00:00:00Z